• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

1. What Amlodipine / Valsartan is and what it is used for
2. What you need to know before you take Amlodipine / Valsartan
3. How to take Amlodipine / Valsartan
4. Possible side effects
5. How to store Amlodipine / Valsartan
6. Contents of the pack and other information

• are allergic to amlodipine or to any other calcium channel blockers. This may involve itching, reddening of the skin or difficulty in breathing.
• are allergic to valsartan or any of the other ingredients of this medicine (listed in section 6). If you think you may be allergic, talk to your doctor before taking Amlodipine / Valsartan.
• have severe liver problems or bile problems such as biliary cirrhosis or cholestasis.
• are more than 3 months pregnant. (It is also better to avoid Amlodipine / Valsartan in early pregnancy, see section “Pregnancy, breast-feeding and fertility”).
• have severe low blood pressure (hypotension).
• have narrowing of the aortic valve (aortic stenosis) or cardiogenic shock (a condition where your heart is unable to supply enough blood to the body).
• suffer from heart failure after a heart attack.
• have diabetes or impaired kidney function and you are treated with a blood pressure lowering medicine containing aliskiren.

If any of the above applies to you, do not take Amlodipine / Valsartan and talk to your doctor.

Talk to your doctor before taking Amlodipine / Valsartan if

• you have been sick (vomiting or diarrhoea).
• you have liver or kidney problems.
• you have had a kidney transplant or if you had been told that you have a narrowing of your kidney arteries.
• you have a condition affecting the renal glands called “primary hyperaldosteronism”.
• you have had heart failure or have experienced a heart attack. Follow your doctor’s instructions for the starting dose carefully. Your doctor may also check your kidney function.
• your doctor has told you that you have a narrowing of the valves in your heart (called “aortic or mitral stenosis”) or that the thickness of your heart muscle is abnormally increased (called “obstructive hypertrophic cardiomyopathy”).
• you have experienced swelling, particularly of the face and throat, while taking other medicines (including angiotensin converting enzyme inhibitors). If you get these symptoms, stop taking Amlodipine / Valsartan and contact your doctor straight away. You should never take Amlodipine / Valsartan again.
• you are taking any of the following medicines used to treat high blood pressure:
  • an ACE inhibitor (for example enalapril, lisinopril, ramipril), in particular if you have diabetes-related kidney problems.
  • aliskiren.

Your doctor may check your kidney function, blood pressure, and the amount of electrolytes (e.g. potassium) in your blood at regular intervals.

See also information under the heading “Do not take Amlodipine / Valsartan”.

If any of these apply to you, tell your doctor before taking Amlodipine / Valsartan.

The use of Amlodipine / Valsartan in children and adolescents is not recommended (aged below 18 years old).

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Your doctor may need to change your dose and/or to take other precautions. In some cases you may have to stop taking one of the medicines. This applies especially to the medicines listed below:

• ACE inhibitors or aliskiren (see also information under the headings “Do not take Amlodipine / Valsartan” and “Warnings and precautions”).
• diuretics (a type of medicine also called “water tablets” which increases the amount of urine you produce)
• lithium (a medicine used to treat some types of depression).
• potassium-sparing diuretics, potassium supplements, salt substitutes containing potassium and other substances that may increase potassium levels.
• certain types of painkillers called non-steroidal anti-inflammatory medicines (NSAIDs) or selective cyclooxygenase-2 inhibitors (COX-2 inhibitors).
  Your doctor may also check your kidney function.
• anticonvulsant agents (e.g. carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidone).
• St. John’s Wort.
• nitroglycerin and other nitrates, or other substances called “vasodilators”.
• medicines used for HIV/AIDS (e.g. ritonavir, indinavir, nelfinavir).
• medicines used to treat fungal infections (e.g. ketoconazole, itraconazole).
• rifampicin, erythromycin, clarithromycin, talithromycin (antibiotics – for infections caused by bacteria)
• verapamil, diltiazem (heart medicines).
• tacrolimus (used to control your body’s immune response, enabling your body to accept the transplanted organ).
• simvastatin (a medicine used to control high cholesterol levels).
• dantrolene (infusion for severe body temperature abnormalities).
• medicines used to protect against transplant rejection (ciclosporin).

Grapefruit and grapefruit juice should not be consumed by people who are taking Amlodipine / Valsartan.

This is because grapefruit and grapefruit juice can lead to an increase in the blood levels of the active substance amlodipine, which can cause an unpredictable increase in the blood pressure lowering effect of Amlodipine / Valsartan.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Pregnancy

You must tell your doctor if you think you are (or might become) pregnant. Your doctor will normally advise you to stop taking Amlodipine / Valsartan before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Amlodipine / Valsartan. Amlodipine / Valsartan is not recommended in early pregnancy (first 3 months), and must not be taken when more than 3 months pregnant, as it may cause serious harm to your baby if used after the third month of pregnancy.

Breast-feeding

Amlodipine has been shown to pass into breast milk in small amounts. If you are breast-feeding or about to start breast-feeding you must tell your doctor before taking Amlodipine/ Valsartan. Amlodipine / Valsartan is not recommended for mothers who are breast-feeding, and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is new-born, or was born prematurely.

This medicine may make you feel dizzy. This can affect how well you can concentrate. So, if you are not sure how this medicine will affect you, do not drive, use machinery, or do other activities that you need to concentrate on.

Amlodipine / Valsartan 5 mg / 80 mg film-coated tablets: This medicine contains 9.25 mg sorbitol in each tablet.

Amlodipine / Valsartan 5 mg / 160 mg film-coated tablets and Amlodipine / Valsartan 10 mg / 160 mg film-coated tablets:

This medicine contains 18.5 mg sorbitol in each tablet.

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.

Your doctor should exercise caution when increasing your dose.

If you have taken too many tablets of Amlodipine / Valsartan, or if someone else has taken your tablets, consult a doctor immediately.

Excess fluid may accumulate in your lungs (pulmonary oedema) causing shortness of breath that may develop up to 24-48 hours after intake.

If you forget to take this medicine, take it as soon as you remember. Then take your next dose at its usual time. However, if it is almost time for your next dose, skip the dose you missed. Do not take a double dose to make up for a forgotten tablet.

Stopping your treatment with Amlodipine / Valsartan may cause your disease to get worse. Do not stop taking your medicine unless your doctor tells you to.

A few patients have experienced these serious side effects (may affect up to 1 in 1,000 people). If any of the following happen, tell your doctor straight away:

Allergic reaction with symptoms such as rash, itching, swelling of face or lips or tongue, difficulty breathing, low blood pressure (feeling of faintness, light-headedness).

Common (may affect up to 1 in 10 people):

Influenza (flu); blocked nose, sore throat and discomfort when swallowing; headache; swelling of arms, hands, legs, ankles or feet; tiredness; asthenia (weakness); redness and warm feeling of the face and/or neck.

Uncommon (may affect up to 1 in 100 people):

Dizziness; nausea and abdominal pain; dry mouth; drowsiness, tingling or numbness of the hands or feet; vertigo; fast heart beat including palpitations; dizziness on standing up; cough; diarrhoea; constipation; skin rash, redness of the skin; joint swelling, back pain; pain in joints.

Rare (may affect up to 1 in 1,000 people):

Feeling anxious; ringing in the ears (tinnitus); fainting; passing more urine than normal or feeling more of an urge to pass urine; inability to get or maintain an erection; sensation of heaviness; low blood pressure with symptoms such as dizziness, light-headedness; excessive sweating; skin rash all over your body; itching; muscle spasm.

If any of these affect you severely, tell your doctor.

Side effects reported with amlodipine or valsartan alone and either not observed with Amlodipine / Valsartan or observed with a higher frequency than with Amlodipine / Valsartan.

Consult a doctor immediately if you experience any of the following very rare, severe side effects after taking this medicine:

• sudden wheeziness, chest pain, shortness of breath or difficulty in breathing.
• swelling of eyelids, face or lips.
• swelling of the tongue and throat which causes great difficulty breathing.
• severe skin reactions including intense skin rash, hives, reddening of the skin over your whole body, severe itching, blistering, peeling and swelling of the skin, inflammation of the mucous membranes (Stevens- Johnson Syndrome, toxic epidermal necrolysis) or other allergic reactions.
• heart attack, abnormal heart beat.
• inflamed pancreas, which may cause severe abdominal and back pain accompanied with feeling of being very unwell.

The following side effects have been reported. If any of these cause you problems or if they last for more than one week, you should contact your doctor.

Common (may affect up to 1 in 10 people): Dizziness, sleepiness; palpitations (awareness of your heart beat); flushing, ankle swelling (oedema); abdominal pain, feeling sick (nausea).

Uncommon (may affect up to 1 in 100 people): Mood changes, anxiety, depression, sleeplessness, trembling, taste abnormalities, fainting, loss of pain sensation; visual disturbances, visual impairment, ringing in the ears; low blood pressure; sneezing/runny nose caused by inflammation of the lining of the nose (rhinitis); indigestion, vomiting (being sick); hair loss, increased sweating, itchy skin, skin discolouration; disorder in passing urine, increased need to urinate at night, increased number of times of passing urine; inability to obtain an erection, discomfort or enlargement of the breasts in men, pain, feeling unwell, muscle pain, muscle cramps; weight increase or decrease.

Rare (may affect up to 1 in 1,000 people): Confusion.

Very rare (may affect up to 1 in 10,000 people):

Decreased number of white blood cells, decrease in blood platelets which may result in unusual bruising or easy bleeding; excess sugar in blood (hyperglycaemia); swelling and/or bleeding of the gums, abdominal bloating (gastritis); abnormal liver function, inflammation of the liver (hepatitis), yellowing of the skin (jaundice), liver enzyme increase which may have an effect on some medical tests; increased muscle tension; inflammation of blood vessels often with skin rash, sensitivity to light.

Not known (frequency cannot be estimated from the available data):

Trembling, rigid posture, mask-like face, slow movements and a shuffling, unbalanced walk.

Not known (frequency cannot be estimated from the available data):

Decrease in red blood cells, fever, sore throat or mouth sores due to infections; spontaneous bleeding or bruising; high level of potassium in the blood; abnormal liver test results; decreased renal functions and severely decreased renal functions; swelling mainly of the face and the throat; muscle pain; rash, purplish-red spots; fever; itching; allergic reaction, blistering skin (sign of a condition called dermatitis bullous).

If you experience any of these, tell your doctor straight away.

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly the Yellow card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

By reporting side effects, you can help provide more information on the safety of this medicine.

• The active substance are amlodipine and valsartan.
  Amlodipine / Valsartan 5 mg / 80 mg film-coated tablets
  Each film-coated tablet contains 5 mg amlodipine (as amlodipine besilate) and 80 mg valsartan.
  Amlodipine / Valsartan 5 mg / 160 mg film-coated tablets
  Each film-coated tablet contains 5 mg amlodipine (as amlodipine besilate) and 160 mg valsartan.
  Amlodipine / Valsartan 10 mg / 160 mg film-coated tablets
  Each film-coated tablet contains 10 mg amlodipine (as amlodipine besilate) and 160 mg valsartan.
• The other ingredients are: Tablet core: silicified microcrystalline cellulose (containing cellulose microcrystalline and silica colloidal anhydrous); sorbitol (E420); magnesium carbonate; starch pregelatinised; pregelatinised starch, partially; povidone 25; sodium stearyl fumarate; sodium lauryl sulphate; crospovidone type A; silica colloidal anhydrous; cellulose microcrystalline.
  Tablet coating: hypromellose 2910/5; macrogol 6000; titanium dioxide (E171); talc; yellow ferric oxide (E172).

Amlodipine / Valsartan 5 mg / 80 mg film-coated tablets:

Yellow rounded film-coated tablet of dimension approx. 9 mm.

Amlodipine / Valsartan 5 mg / 160 mg film-coated tablets:

Light yellow oblong film-coated tablet of dimension approx. 14×7 mm.

Amlodipine / Valsartan 10 mg / 160 mg film-coated tablets:

Yellow oblong film-coated tablet with break line, dimension approx. 14×7 mm.

7, 14, 28, 30, 56, 90, 98 film-coated tablets.

Not all pack sizes may be marketed.